A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733546



Internal ID157212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62068239..62068277hg38UCSC Ensembl
chr20:60643295..60643333hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733546
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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